Inoculation of lactating ewes by the intramammary route with Mycoplasma agalactiae: comparative pathogenicity of six field strains
Vet. Res., 31 3 (2000) 329-337
Articles citing this article
The Citing articles tool gives a list of articles citing the current article.
The citing articles come from EDP Sciences database, as well as other publishers participating in CrossRef Cited-by Linking Program. You can set up your personal account to receive an email alert each time this article is cited by a new article (see the menu on the right-hand side of the abstract page).
Cited article:
This article has been cited by the following article(s):
Mycoplasma agalactiae Vaccines: Current Status, Hurdles, and Opportunities Due to Advances in Pathogenicity Studies
Maysa Santos Barbosa, Beatriz Almeida Sampaio, Joachim Spergser, Renate Rosengarten, Lucas Miranda Marques and Rohini Chopra-DewasthalyVaccines 12 (2) 156 (2024)
https://doi.org/10.3390/vaccines12020156
Influence of natural and climatic conditions on the distribution and forms of contagious agalactia in sheep in Bessarabia, Ukraine
Mykola Volodymyrovych Bohach, Vitaliy Igorovych Bolotin, Denys Mykolaivych Bohach, Olha Tarasivna Piven and Iryna Victorivna PyvovarovaJournal of Veterinary Research 66 (3) 345 (2022)
https://doi.org/10.2478/jvetres-2022-0047
https://doi.org/10.1079/cabicompendium.74530
https://doi.org/10.1079/cabicompendium.74487
Can vaccines for contagious agalactia reduce disease progression in infected animals: a preliminary study?
Guido Ruggero Loria, Roberto Puleio, Stefano Agnello, Gavino Marogna and Robin A J NicholasVeterinary Record Case Reports 6 (4) (2018)
https://doi.org/10.1136/vetreccr-2018-000715
Detecting asymptomatic rams infected with Mycoplasma agalactiae in ovine artificial insemination centers
Miranda Prats-van der Ham, Juan Tatay-Dualde, Christian de la Fe, et al.Theriogenology 89 324 (2017)
https://doi.org/10.1016/j.theriogenology.2016.09.014
Simultaneous Identification of Potential Pathogenicity Factors of Mycoplasma agalactiae in the Natural Ovine Host by Negative Selection
Shivanand Hegde, Shrilakshmi Hegde, Martina Zimmermann, et al.Infection and Immunity 83 (7) 2751 (2015)
https://doi.org/10.1128/IAI.00403-15
Ultrasound and histopathological investigations of experimentally induced Staphylococcus aureus mastitis in goats
Ivan Fasulkov, Manol Karadaev, Nasko Vasilev, et al.Small Ruminant Research 129 114 (2015)
https://doi.org/10.1016/j.smallrumres.2015.05.018
Experimental Infections with Mycoplasma agalactiae Identify Key Factors Involved in Host-Colonization
Eric Baranowski, Dominique Bergonier, Eveline Sagné, et al.PLoS ONE 9 (4) e93970 (2014)
https://doi.org/10.1371/journal.pone.0093970
Anatomic location of Mycoplasma mycoides subsp. capri and Mycoplasma agalactiae in naturally infected goat male auricular carriers
Ángel Gómez-Martín, Christian De la Fe, Joaquín Amores, et al.Veterinary Microbiology 157 (3-4) 355 (2012)
https://doi.org/10.1016/j.vetmic.2012.01.004
Unexpected genetic diversity of Mycoplasma agalactiae caprine isolates from an endemic geographically restricted area of Spain
Christian De la Fe, Joaquín Amores, Florence Tardy, et al.BMC Veterinary Research 8 (1) 146 (2012)
https://doi.org/10.1186/1746-6148-8-146
Role of Vpma phase variation inMycoplasma agalactiaepathogenesis
Rohini Chopra-Dewasthaly, Martina Baumgartner, Erika Gamper, et al.FEMS Immunology & Medical Microbiology 66 (3) 307 (2012)
https://doi.org/10.1111/j.1574-695X.2012.01010.x
Chronological and immunohistochemical characterization of the mammary immunoinflammatory response in experimental caprine contagious agalactia
Ayoze Castro-Alonso, Christian De la Fe, Antonio Espinosa de los Monteros, et al.Veterinary Immunology and Immunopathology 136 (1-2) 43 (2010)
https://doi.org/10.1016/j.vetimm.2010.02.005
Correlating the immune response with the clinical–pathological course of persistent mastitis experimentally induced by Mycoplasma agalactiae in dairy goats
A. Castro-Alonso, F. Rodríguez, C. De la Fé, et al.Research in Veterinary Science 86 (2) 274 (2009)
https://doi.org/10.1016/j.rvsc.2008.06.004
Presence of Mycoplasma species and somatic cell counts in bulk-tank goat milk
A. Contreras, R.E. Miranda, A. Sánchez, et al.Small Ruminant Research 75 (2-3) 247 (2008)
https://doi.org/10.1016/j.smallrumres.2007.11.007
Jubb, Kennedy & Palmer's Pathology of Domestic Animals
Jubb, Kennedy & Palmer's Pathology of Domestic Animals 563 (2007)https://doi.org/10.1016/B978-070202823-6.50195-0
Contagious agalactia in small ruminants
J.C. Corrales, A. Esnal, C. De la Fe, et al.Small Ruminant Research 68 (1-2) 154 (2007)
https://doi.org/10.1016/j.smallrumres.2006.09.010
Comparison of four diagnostic tests for the identification of serum antibodies in small ruminants infected withMycoplasma agalactiae
R Kittelberger, JS O'Keefe, R Meynell, et al.New Zealand Veterinary Journal 54 (1) 10 (2006)
https://doi.org/10.1080/00480169.2006.36597
Effect of Clinical Contagious Agalactia on the Bulk Tank Milk Somatic Cell Count in Murciano-Granadina Goat Herds
J.C. Corrales, A. Sánchez, C. Luengo, J.B. Poveda and A. ContrerasJournal of Dairy Science 87 (10) 3165 (2004)
https://doi.org/10.3168/jds.S0022-0302(04)73451-7
Comparison of Three Enzyme-Linked Immunosorbent Assays for Serologic Diagnosis of Contagious Agalactia in Sheep
Michel Pépin, Philippe Dufour, Maurice Lambert, Michel Aubert, Aurèle Valognes, Thierry Rotis, Anne Van de Wiele and Dominique BergonierJournal of Veterinary Diagnostic Investigation 15 (3) 281 (2003)
https://doi.org/10.1177/104063870301500311
Prevalence and distribution of the insertion element ISMag1 in Mycoplasma agalactiae
Paola Pilo, Bénédicte Fleury, Marc Marenda, Joachim Frey and Edy M. VileiVeterinary Microbiology 92 (1-2) 37 (2003)
https://doi.org/10.1016/S0378-1135(02)00311-5
Molecular Biology and Pathogenicity of Mycoplasmas
Joachim FreyMolecular Biology and Pathogenicity of Mycoplasmas 73 (2002)
https://doi.org/10.1007/0-306-47606-1_4